1200-84-6

Upstream product

• 505-14-6 thiocyanogen 
• 824-79-3 sodium 4-methylbenzenesulfinate 

Downstream Products

• 80120-55-4 1-(p-tolylsulfonyl)-4-thiocynato-2-butene 
• 77825-82-2 2-(p-Toluenesulfonyl)indene 
• 80120-68-9 1-(p-tolylsulfonyl)-2,3-dimethyl-1,3-butadiene 
• 80120-67-8 2-(p-tolylsulfonylmethyl)-3-methyl-1,3-butadiene 
• 212063-23-5 2-methyl-1-(p-toluenesulfonyl)-1,3-butadiene 
• 115125-84-3 1-Methyl-4-[((1Z,3E)-penta-1,3-diene)-1-sulfonyl]-benzene 
• 108320-21-4 1-toluenesulfonylbuta-1,3-diene 
• 115125-86-5 1-p-tolylsulphonylcyclohexa-1,3-diene 
• 64472-72-6 1-((1Z,3Z)-5,5-Dimethyl-hexa-1,3-diene-1-sulfonyl)-4-methyl-benzene 
• 80120-62-3 1-Methyl-4-((E)-2-methyl-4-thiocyanato-but-2-ene-1-sulfonyl)-benzene 
• 80120-65-6 1-(p-tolylsulfonyl)-4-thiocyanato-2,3-dimethyl-2-butene 
• 80120-64-5 1-((E)-5,5-Dimethyl-4-thiocyanato-hex-2-ene-1-sulfonyl)-4-methyl-benzene 
• 80120-63-4 1-Methyl-4-((E)-4-thiocyanato-pent-2-ene-1-sulfonyl)-benzene 
• 10079-12-6 1-Methyl-4-(2-thiocyanato-cyclohexanesulfonyl)-benzene 

Relevant academic research and scientific papers

REACTION OF 1,3-DIENES WITH ARYLSULFONYL THIOCYANATES

At room temperature arylsulfonyl thiocyanates add to conjugated dienes with the formation of 1,4-addition products.In all cases the organic sulfonyl radical is fixed at the least substituted carbon atom of the 1,3-diene system.In reaction with triethylamine or sodium ethoxide the adducts which form eliminate thiocyanic acid with the formation of conjugated dienyl sulfones.